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Update on genetics research

Update on genetics research. Dennis Drayna, PhD NIDCD/National Institutes of Health US Public Health Service, DHHS. Who are we?. National Institute on Deafness and Other Communication Disorders National Institutes of Health U.S. Public Health Services

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Update on genetics research

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  1. Update on genetics research Dennis Drayna, PhD NIDCD/National Institutes of Health US Public Health Service, DHHS

  2. Who are we? • National Institute on Deafness and Other Communication Disorders • National Institutes of Health • U.S. Public Health Services • U.S. Department of Health and Human Services • Your tax dollars at work

  3. Fact #1- Not all stuttering is genetic • Of the people who come to stuttering therapy, about half report a family history and half have no family history • So, perhaps half of stuttering is due to genetic factors • The other half is due to unknown causes • Low birth weight, perinatal hypoxia

  4. Fact #2 - Genes do not entirely control stuttering in anyone • Severity varies from day to day, and in children, from month to month • Stuttering therapy can largely eliminate stuttering • Their genes have not changed

  5. The power of genetics • If a disorder is genetic in origin, we can find the gene that causes the disorder • Once we have the gene, we can see what the gene codes for, and what the gene product does, both normally and in individuals who stutter • Can lead us to the cells and molecules involved in the disorder

  6. Genetics is great, but… • How do we know stuttering has anything to do with genetics? • Nature vs. nurture

  7. Evidence for genetic factors in stuttering • Twin studies • Identical twins always more alike regarding stuttering than fraternal twins • Adoption studies • Adopted children raised by stuttering parents do not stutter any more than children in the general population • Family clusters of stuttering • Several large families have been described that have many, often distantly related members who stutter • Segregation analysis • Stuttering does not generally occur in families like a simple inherited trait

  8. NIH genetics research • Genetic linkage studies • Performed in families • Applicable to any inherited disorder • Identify the location of the gene or genes that cause the disorder

  9. Focus • Persistent stuttering • Family history of stuttering

  10. NIH linkage studies • North American families • Not very enlightening • West African families • Pakistani families

  11. Cameroon, West Africa • Initial contact came through the online symposium sponsored by Stuttering Home Page • Query from individual in Cameroon • Initial information difficult to interpret • Subsequent exam at the N.I.H. Clinical Center showed no medical abnormalities except stuttering

  12. Linkage studies – Cameroon

  13. Cameroon Family 1

  14. Cameroon linkageThe long march • Did one survey and found a signal on chromosome 1 • Did not replicate • Did two additional surveys, using two different methods • Took ~ 2 years of work • Found clear signal on chromosome 15

  15. Cameroon linkage • Linkage on chromosome 15 still has puzzling aspects • There’s likely to be more than one variant gene at this location at work in this family • Don’t yet know what this gene is

  16. Linkage studies - Pakistan

  17. Pakistani stuttering familiesPKST 072

  18. Pakistan project • Enrolled and analyzed 44 families • Found strong evidence for linkage on chromosome 12 • This region contains 87 genes • Analyzed these genes in: • Family PKST 72 • Other Pakistani stuttering families • 96 unrelated Pakistanis who stutterer • 96 unrelated normally fluent Pakistanis

  19. New Results • In review at a major scientific journal • Nothing is true until the reviewers and editors at the journal say it’s true • All information strictly embargoed prior to publication

  20. Results of gene analysis • Found mutation that went along with stuttering in family PKST 72 • Same mutation in the same gene is present in affected members (but not in normal members) of 3 other Pakistani stuttering families • Same mutation in the same gene is observed in several unrelated Pakistani individuals who stutter • Same mutation was observed in a single affected individual of Indian descent in the U.S. • This mutation was not observed in normally fluent individuals

  21. Chromosome 12 gene analysis • Examined the entire gene in: • 96 unrelated Pakistani affected individuals • 270 unrelated North American affected individuals • 96 unrelated normally fluent Pakistanis • 265 unrelated normally fluent North Americans • All have a family history of stuttering • Found several other mutations in this gene that occur in individuals who stutter but do not occur in normally fluent individuals

  22. Looking beyond chromosome 12 • The chromosome 12 gene is part of a well-known process within the body • A metabolic pathway • Other parts of this process are carried out by the products of other well-known genes

  23. Examining other genes • Found a number of mutations in each of two other genes • These mutations were found in multiple individuals who stutter • These mutations were not found in normally fluent individuals

  24. How common? • Together, the mutations we’ve found in these three genes appear to account for 5-10% of familial stuttering • This amounts to 50,000 to 100,000 individuals in the U.S. • Mutations in these genes probably account for many more individuals who stutter worldwide

  25. What’s next? • These genes provide an exciting possibility for therapy in this group of individuals • Replace what’s missing • Personalized medicine • Making a new drug takes many years and many hundreds of millions of dollars • Can’t expect a cure next week

  26. What about the other 90%? • Studies have shown that genetics works • Enrolled a new group of Pakistani stuttering families, each of which is large enough to be useful for a linkage study on its own • Chromosome 12 has already been ruled out in these families • Likely to find other places containing stuttering genes • Chromosome 15 will hopefully identify another new gene

  27. Current conclusions • Studies have shown that genetics works • There’s good hope for finding other genes that cause stuttering, leading to additional insights • At least some stuttering is clearly in the realm of clinical medicine

  28. Acknowledgments • NIDCD • Changsoo Kang • M. Hashim Raza • Naveeda Riaz • Eduardo Sainz • Joe Kleinman • NISC/NHGRI • Alice Young • Jim Mullikan • NCBI • Alejandro Schaffer • Hollins Communications Research Institute • Jennifer Mundorff • University of Chicago • Stacy Steinberg • Anna Pluzhnikov • Nancy Cox • CEMB/University of the Punjab • Jamil Ahmad • Shahid Khan • S. Riazuddin • Stuttering Foundation of America • British Stammering Association • National Stuttering Association • Speak Clear Association of Cameroon • Joseph Lukong • Stuttering research subjects worldwide

  29. How do we make progress? • You can help! • Enrolling research subjects here today, immediately following this workshop • Compensation provided

  30. What’s needed? • Family history of stuttering • Provide a small blood sample, taken from your arm • Understand and agree to the risks involved • Provide a Social Security number to receive your compensation • $25

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